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Fig. 7 | Hereditary Cancer in Clinical Practice

Fig. 7

From: Preoperative multimodal ultrasonic imaging in a case of Peutz-Jeghers syndrome complicated by atypical lobular endocervical glandular hyperplasia: a case report and literature review

Fig. 7

Sequencing results for STK11 in the patient and her family members. Whole-exome sequencing (patient) and Sanger sequencing (patient’s father and brother) confirmed the pathogenic heterogeneous mutation of the STK11 gene mapped to Chr19:1207063–1,207,063, NM_000455.5:exon1:.150dup (p.Met51Aspfs*112)

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Hereditary Cancer in Clinical Practice

ISSN: 1897-4287